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"68180-211-03" National Drug Code (NDC)
Losartan Potassium 1000 TABLET in 1 BOTTLE (68180-211-03)
(Lupin Pharmaceuticals, Inc.)
NDC Code
68180-211-03
Package Description
1000 TABLET in 1 BOTTLE (68180-211-03)
Product NDC
68180-211
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Losartan Potassium
Non-Proprietary Name
Losartan Potassium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20101006
End Marketing Date
20190131
Marketing Category Name
ANDA
Application Number
ANDA078232
Manufacturer
Lupin Pharmaceuticals, Inc.
Substance Name
LOSARTAN POTASSIUM
Strength
50
Strength Unit
mg/1
Pharmacy Classes
Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68180-211-03